US4187080A - Treating condensate from gasification of coal - Google Patents

Treating condensate from gasification of coal Download PDF

Info

Publication number
US4187080A
US4187080A US05/840,433 US84043377A US4187080A US 4187080 A US4187080 A US 4187080A US 84043377 A US84043377 A US 84043377A US 4187080 A US4187080 A US 4187080A
Authority
US
United States
Prior art keywords
solids
condensate
gasification
tar
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US05/840,433
Inventor
Carl Hafke
Roland Weber
Rudolf Kohlen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GEA Group AG
Original Assignee
Metallgesellschaft AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE2607745A external-priority patent/DE2607745C2/en
Application filed by Metallgesellschaft AG filed Critical Metallgesellschaft AG
Priority to US05/840,433 priority Critical patent/US4187080A/en
Application granted granted Critical
Publication of US4187080A publication Critical patent/US4187080A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/72Other features
    • C10J3/82Gas withdrawal means
    • C10J3/84Gas withdrawal means with means for removing dust or tar from the gas
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/02Fixed-bed gasification of lump fuel
    • C10J3/20Apparatus; Plants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/72Other features
    • C10J3/78High-pressure apparatus
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913Carbonaceous raw material
    • C10J2300/093Coal
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913Carbonaceous raw material
    • C10J2300/0946Waste, e.g. MSW, tires, glass, tar sand, peat, paper, lignite, oil shale
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953Gasifying agents
    • C10J2300/0959Oxygen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953Gasifying agents
    • C10J2300/0973Water
    • C10J2300/0976Water as steam
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/1807Recycle loops, e.g. gas, solids, heating medium, water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/1861Heat exchange between at least two process streams
    • C10J2300/1884Heat exchange between at least two process streams with one stream being synthesis gas
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/1861Heat exchange between at least two process streams
    • C10J2300/1892Heat exchange between at least two process streams with one stream being water/steam

Definitions

  • This invention relates to a process of treating condensate formed by a cooling of raw gas produced from solid fuels by a pressure gasification comprising a treatment with oxygen and water vapor.
  • Carbon dioxide may be used as a further gasifying agent.
  • the solid fuels which are suitable for pressure gasification include mainly coal, brown coal, and peat. It is basically known to gasify such solid fuels under operating pressures in the range of about 5-150 bars, preferably about 10-80 bars.
  • the pressure gasification can be carried out with particularly good results in the Lurgi gas-producing reactor, details of which are described in Printed German Application No. 1,021,116, German Patent No. 2,352,900, and U.S. Pat. Nos. 3,540,867; 3,902,872; and 3,930,811, the disclosure of which are incorporated herein by reference.
  • the known pressure gasification process results in a raw gas, which leaves the pressure reactor at temperatures in the range of about 400°-700° C. and which contains on a dry basis about 20-80% water vapor and about 1-10 g finegrained solids per standard cubic meter.
  • Tests have shown that the particle size range of the solids entrained by the raw gas depends highly on the space velocity in the reactor. It has been found that the gasification of caking coals and particularly also of swelling coal results in a discharge of more solids than the gasification of non-caking and non-swelling coals.
  • the solids consist mainly of unreacted fuel and of ash particles.
  • the raw gas discharged from the pressure reactor is first scrubbed in direct contact with water and cooled condensate. This scrubbing results in a removal of solids and in a condensation of part of the hydrocarbons, tars and water vapor.
  • pumpable condensates may no longer be formed after a short time of operation. It is also known that the processing of caking and swelling coals can be much improved in that the mixture which is obtained after the cooling of the raw gas and which contains tars, hydrocarbons, and solids, is recycled at least in part to the pressure gasification process.
  • the pressure gasification reactors can be operated at a high throughput rate of about 10-20 metric tons of fuel per hour. This results in an increase of the absolute quantities of solids entrained by the raw gas and also in a larger average particle diameter of said solids. After a certain time of operation these phenomena may result in disturbances in the conduit and pump system.
  • screens were used to separate the coarse-grained solids from the condensate mixture have not given satisfactory results because these coarse separators must be cleaned at a considerable expenditure. The coarse particles which are thus removed still contain high boiling tars and must be destroyed at a considerable expenditure because discarding of such solids is not permissible for ecological reasons.
  • the high-solids fraction derived from the condensate mixture no longer contains any substantial quantity of coarse particles having a size above 2 mm.
  • the processing in the solids disintegrator results also in a mixing of the particles in the condensate to a certain degree and in a homogenization of the mixture. It has been found that the processed mixture no longer tends to form disturbing deposits, particularly in conduits and pumps.
  • the condensate which is recycled to the pressure gasification process and the condensate which is fed to the separator are suitably kept at a temperature above about 50° C., preferably above about 70° C.
  • the increased temperature prevents solidification of the tar constituents in the condensate.
  • Such solidified tar constituents could promote adhesion of deposits and clogging.
  • the high-solids heavy fraction withdrawn from the separator may have a solids content of about 10-60%. This mixed fraction can be handled without trouble even when its solids content is close to or at said upper limit.
  • the processing of the condensate in the solids disintegrator is suitably controlled so that a predominant part of the solids in the processed condensate has a particle size below about 0.5 mm. Solids having a small particle size can be more easily maintained in a state of fine division in the tar-containing condensate so that they will not give rise to any trouble.
  • Granular solid fuel is fed to a pressure gasification reactor 1 through a conduit 2.
  • the reactor 1 is fed with oxygen-containing gas through conduit 3 and with water vapor through conduit 4.
  • the ash left after the gasification is withdrawn in conduit 5.
  • the raw gas produced by the gasification flows at temperatures of about 400°-700° C. from the reactor 1 into a scrubber-cooler 7 and is directly contacted therein with a mixture of water and condensate at temperatures of about 160°-220° C. Scrubbed gas which is saturated with water vapor is conducted in conduit 8 to a waste-heat boiler 9.
  • part of the condensate collected in the scrubber-cooler 7 is added to the water-heat boiler.
  • the gas which has been cooled in the waste-heat boiler leaves the latter through conduit 11.
  • Condensate collected in the sump of the waste-heat boiler is returned through conduit 12 to the scrubber-cooler 7.
  • Fresh water is added through conduit 13.
  • the gas having a saturation temperature of 160°-180° C. must be purified further and used, e.g., in a combined gas-steam turbine process. In such case, the waste-heat boiler may be eliminated and the saturated gas leaving the scrubber-cooler is fed to any purification stages which may be required.
  • a condensate mixture which contains the solids that have been removed from the raw gas in the scrubber-cooler 7 is discharged in conduit 15 and is pressure-relieved in atmospheric pressure in one or more pressure-relief stages.
  • the pressure-relieved mixture is fed to a separator 17, in which the several constitutents of the mixture are separated by gravity.
  • a major portion of the solids mainly together with heavy, high-boiling tar, is collected in the lowermost part of the separator 17.
  • Hydrocarbons, lower-boiling tars and oil are enriched in an intermediate portion above said solids; these constituents contain only little dust and are fed through conduit 18 to means for their further processing.
  • the upper part of the gravity separator 17 contains a mixture which comprises aqueous condensate, light hydrocarbons and light oils. This mixture is withdrawn through withdrawal conduit 19. Pressure-relieved gas leaves the separator through conduit 20.
  • the high-solids heavy fraction separated in the separator 17 is fed from the lower end of the separator through conduit 21 to a disintegrator 22.
  • the solids are embedded in a vehicle of high viscosity and are disintegrated in the disintegrator 22 to a final particle size upper limit of about 2 mm.
  • the disintegration of the solids results also in a homogenization of the mixture as it passes through the disintegrator.
  • Suitable disintegrators are, e.g., dispersing machines known for the production of pharmaceuticals (Ullmann's Encyklopadie der ischen Chemie, Vol. 4 (1953), pages 21/22).
  • At least part of the solids-containing condensate discharged from the disintegrator 22 is fed by pump 23 through conduit 24 and by a metering pump 25 through conduit 26 and is thus recycled into the upper portion of the pressure gasification reactor 1.
  • the surplus of the condensate mixture is recycled through conduit 27 to the separator 17 and is fed thereto either through a conduit 28, which includes a valve 29, or through a conduit 30, which includes a valve 31.
  • conduit 27 is foreseen in which the flow can be adjusted by valve 29 or 31.
  • the amount of flow in conduit 27 should be about 20-60% of the amount of mixture normally withdrawn from separator 17 by conduit 21.
  • the flow rate in conduit 27 should be at least 10% of the normal feed rate in conduit 26 and may be increased in order to adjust the ratio of dust and tar in the mixture withdrawn from separator 17 by conduit 21.
  • feeding part of the mixture back to separator 17 via conduit 27 may be advantageous, it is not an essential feature of the process.
  • a Lurgi gas-producing reactor 1 operated at an output rate of 2000 standard m 3 /h moist raw gas per m 2 of the inside cross-sectional area of the reactor was fed with coal having the following specification:
  • the pressure gasification reactor is operated under a pressure of 20 bars and discharges a raw gas which is at a temperature of 550° C.
  • the raw gas is cooled to 180° C. in the scrubber-cooler.
  • a tar- and dust-containing condensate mixture is fed to a gravity separator 17, from the lower end of which a high-solids heavy fraction is withdrawn.
  • the solids have an average particle diameter of about 1.5 mm and the mixture has a solids content of 20% by weight.
  • the commercially available pumps used to recycle the mixture to the pressure reactor 1 and to recycle the mixture through corduit 27 failed after about 10 hours of operation so that the gasification then had to be stopped. When screens were installed in conduit 21, gas could be produced for a longer time but a tar- solids mixture had to be removed from the plant and destroyed at a rate of 100 liters per hour and per pressure reactor.
  • Example 1 The same gas producer as in Example 1 was operated at an output rate of 5000 standard m 3 /h raw gas per m 2 of the inside cross-sectional area of the reactor, i.e., at 21/2 times the output rate in Example 1.
  • the feed coal and the significant operating conditions were the same as in Example 1.
  • the higher output rate had the result that the average particle diameter of the solids contained in the raw gas increased to 5 mm. Because the process was carried out as shown in the drawing and included the use of the solids disintegrator 22, the solids in the mixture conducted in conduit 21 were disintegrated substantially to a particle size upper limit of 2 mm. The average particle diameter was about 0.5 mm and the condensate mixture had a solids content of 45% by weight. Although solids-containing condensate was not removed from the plant, the gasification could be effected continuously for several months.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Industrial Gases (AREA)

Abstract

In the production of gas from a solid fuel comprising effecting gasification by contacting the solid fuel with oxygen and water under pressure to form raw gas containing tar, solids and water, cooling the raw gas to effect condensation of the tar and water, the condensate containing the solids, separating from the solids-containing condensate a fraction enriched in solids, and disposing of said fraction, the improvement which comprises effecting said disposition by feeding at least part of said fraction to a solids disintegrator wherein the solids are reduced in size, and recycling at least part of the condensate containing disintegrated solids to the gasification step. Disintegration serves to reduce substantially all the particles to below about 2 mm with the predominant part below about 0.5 mm. Part of the condensate may also be recycled to the separation stage and all the recycled condensate is kept above 50° C. to prevent solidification of tars. The process permits continuous operation of a gasification plant without clogging of pipes and pumps such as otherwise necessitate equipment shutdown for cleaning.

Description

This is a continuation of application Ser. No. 704,253, filed July 12, 1976, now abandoned.
BACKGROUND
This invention relates to a process of treating condensate formed by a cooling of raw gas produced from solid fuels by a pressure gasification comprising a treatment with oxygen and water vapor. Carbon dioxide may be used as a further gasifying agent.
The solid fuels which are suitable for pressure gasification include mainly coal, brown coal, and peat. It is basically known to gasify such solid fuels under operating pressures in the range of about 5-150 bars, preferably about 10-80 bars. The pressure gasification can be carried out with particularly good results in the Lurgi gas-producing reactor, details of which are described in Printed German Application No. 1,021,116, German Patent No. 2,352,900, and U.S. Pat. Nos. 3,540,867; 3,902,872; and 3,930,811, the disclosure of which are incorporated herein by reference.
The known pressure gasification process results in a raw gas, which leaves the pressure reactor at temperatures in the range of about 400°-700° C. and which contains on a dry basis about 20-80% water vapor and about 1-10 g finegrained solids per standard cubic meter. Tests have shown that the particle size range of the solids entrained by the raw gas depends highly on the space velocity in the reactor. It has been found that the gasification of caking coals and particularly also of swelling coal results in a discharge of more solids than the gasification of non-caking and non-swelling coals. The solids consist mainly of unreacted fuel and of ash particles.
The raw gas discharged from the pressure reactor is first scrubbed in direct contact with water and cooled condensate. This scrubbing results in a removal of solids and in a condensation of part of the hydrocarbons, tars and water vapor. When the gasification results in a raw gas having a high solids content, pumpable condensates may no longer be formed after a short time of operation. It is also known that the processing of caking and swelling coals can be much improved in that the mixture which is obtained after the cooling of the raw gas and which contains tars, hydrocarbons, and solids, is recycled at least in part to the pressure gasification process.
At the present state of the art relating to the pressure gasification of solid fuels, the pressure gasification reactors can be operated at a high throughput rate of about 10-20 metric tons of fuel per hour. This results in an increase of the absolute quantities of solids entrained by the raw gas and also in a larger average particle diameter of said solids. After a certain time of operation these phenomena may result in disturbances in the conduit and pump system. Experiments in which screens were used to separate the coarse-grained solids from the condensate mixture have not given satisfactory results because these coarse separators must be cleaned at a considerable expenditure. The coarse particles which are thus removed still contain high boiling tars and must be destroyed at a considerable expenditure because discarding of such solids is not permissible for ecological reasons.
For this reason it is an object of the invention so to improve a process of the kind defined first hereinbefore that the disadvantages involved in previous proposals are avoided and a trouble-free and economical operation is ensured. This is accomplished according to the invention in that the condensate, which contains tar, solids, and water, is fed to a separator, a heavy fraction having a high solid content is withdrawn from said separator, at least part of said heavy fraction is processed in a solids disintegrator, part of the processed solids having a particle size substantially below about 2 mm are added to the condensate derived from the raw gas produced by pressure gasification, and another part of the processed solids is recycled to the separator.
After the processing in the solids disintegrator, the high-solids fraction derived from the condensate mixture no longer contains any substantial quantity of coarse particles having a size above 2 mm. The processing in the solids disintegrator results also in a mixing of the particles in the condensate to a certain degree and in a homogenization of the mixture. It has been found that the processed mixture no longer tends to form disturbing deposits, particularly in conduits and pumps.
The condensate which is recycled to the pressure gasification process and the condensate which is fed to the separator are suitably kept at a temperature above about 50° C., preferably above about 70° C. The increased temperature prevents solidification of the tar constituents in the condensate. Such solidified tar constituents could promote adhesion of deposits and clogging. The high-solids heavy fraction withdrawn from the separator may have a solids content of about 10-60%. This mixed fraction can be handled without trouble even when its solids content is close to or at said upper limit.
The processing of the condensate in the solids disintegrator is suitably controlled so that a predominant part of the solids in the processed condensate has a particle size below about 0.5 mm. Solids having a small particle size can be more easily maintained in a state of fine division in the tar-containing condensate so that they will not give rise to any trouble.
An embodiment of the process according to the invention will be explained with reference to the drawing which is a schematic flow sheet.
Granular solid fuel, particularly coal, is fed to a pressure gasification reactor 1 through a conduit 2. The reactor 1 is fed with oxygen-containing gas through conduit 3 and with water vapor through conduit 4. The ash left after the gasification is withdrawn in conduit 5. During the pressure gasification in the reactor 1, the fuel is held in a packed bed and moves opposite to the direction of flow of the gasifying agents oxygen and water vapor. The raw gas produced by the gasification flows at temperatures of about 400°-700° C. from the reactor 1 into a scrubber-cooler 7 and is directly contacted therein with a mixture of water and condensate at temperatures of about 160°-220° C. Scrubbed gas which is saturated with water vapor is conducted in conduit 8 to a waste-heat boiler 9. Through conduit 10, part of the condensate collected in the scrubber-cooler 7 is added to the water-heat boiler. The gas which has been cooled in the waste-heat boiler leaves the latter through conduit 11. Condensate collected in the sump of the waste-heat boiler is returned through conduit 12 to the scrubber-cooler 7. Fresh water is added through conduit 13. In some embodiments, the gas having a saturation temperature of 160°-180° C. must be purified further and used, e.g., in a combined gas-steam turbine process. In such case, the waste-heat boiler may be eliminated and the saturated gas leaving the scrubber-cooler is fed to any purification stages which may be required.
A condensate mixture which contains the solids that have been removed from the raw gas in the scrubber-cooler 7 is discharged in conduit 15 and is pressure-relieved in atmospheric pressure in one or more pressure-relief stages. The pressure-relieved mixture is fed to a separator 17, in which the several constitutents of the mixture are separated by gravity. A major portion of the solids mainly together with heavy, high-boiling tar, is collected in the lowermost part of the separator 17. Hydrocarbons, lower-boiling tars and oil are enriched in an intermediate portion above said solids; these constituents contain only little dust and are fed through conduit 18 to means for their further processing. The upper part of the gravity separator 17 contains a mixture which comprises aqueous condensate, light hydrocarbons and light oils. This mixture is withdrawn through withdrawal conduit 19. Pressure-relieved gas leaves the separator through conduit 20.
The high-solids heavy fraction separated in the separator 17 is fed from the lower end of the separator through conduit 21 to a disintegrator 22. The solids are embedded in a vehicle of high viscosity and are disintegrated in the disintegrator 22 to a final particle size upper limit of about 2 mm. The disintegration of the solids results also in a homogenization of the mixture as it passes through the disintegrator. Suitable disintegrators are, e.g., dispersing machines known for the production of pharmaceuticals (Ullmann's Encyklopadie der technischen Chemie, Vol. 4 (1953), pages 21/22). At least part of the solids-containing condensate discharged from the disintegrator 22 is fed by pump 23 through conduit 24 and by a metering pump 25 through conduit 26 and is thus recycled into the upper portion of the pressure gasification reactor 1. The surplus of the condensate mixture is recycled through conduit 27 to the separator 17 and is fed thereto either through a conduit 28, which includes a valve 29, or through a conduit 30, which includes a valve 31. In case the feed of recycled tar-dust mixture via pump 25 and conduit 26 has to be reduced or even stopped, still a certain amount of flow in the system has to be maintained to avoid separation of solids in the mixture. For this purpose conduit 27 is foreseen in which the flow can be adjusted by valve 29 or 31. If the flow in conduit 26 is completely stopped, the amount of flow in conduit 27 should be about 20-60% of the amount of mixture normally withdrawn from separator 17 by conduit 21. Under normal operation conditions the flow rate in conduit 27 should be at least 10% of the normal feed rate in conduit 26 and may be increased in order to adjust the ratio of dust and tar in the mixture withdrawn from separator 17 by conduit 21. Though feeding part of the mixture back to separator 17 via conduit 27 may be advantageous, it is not an essential feature of the process.
The invention is further described in the following illustrative example.
EXAMPLE 1
A Lurgi gas-producing reactor 1 operated at an output rate of 2000 standard m3 /h moist raw gas per m2 of the inside cross-sectional area of the reactor was fed with coal having the following specification:
______________________________________                                    
Tar content (Fischer analysis)                                            
                      12% by weight                                       
Caking index (according to Damm)                                          
                      12                                                  
Particle size range of coal                                               
                      3-30 mm                                             
Swelling index        4                                                   
______________________________________                                    
The pressure gasification reactor is operated under a pressure of 20 bars and discharges a raw gas which is at a temperature of 550° C. The raw gas is cooled to 180° C. in the scrubber-cooler. A tar- and dust-containing condensate mixture is fed to a gravity separator 17, from the lower end of which a high-solids heavy fraction is withdrawn. The solids have an average particle diameter of about 1.5 mm and the mixture has a solids content of 20% by weight. The commercially available pumps used to recycle the mixture to the pressure reactor 1 and to recycle the mixture through corduit 27 failed after about 10 hours of operation so that the gasification then had to be stopped. When screens were installed in conduit 21, gas could be produced for a longer time but a tar- solids mixture had to be removed from the plant and destroyed at a rate of 100 liters per hour and per pressure reactor.
EXAMPLE 2
The same gas producer as in Example 1 was operated at an output rate of 5000 standard m3 /h raw gas per m2 of the inside cross-sectional area of the reactor, i.e., at 21/2 times the output rate in Example 1. The feed coal and the significant operating conditions were the same as in Example 1.
The higher output rate had the result that the average particle diameter of the solids contained in the raw gas increased to 5 mm. Because the process was carried out as shown in the drawing and included the use of the solids disintegrator 22, the solids in the mixture conducted in conduit 21 were disintegrated substantially to a particle size upper limit of 2 mm. The average particle diameter was about 0.5 mm and the condensate mixture had a solids content of 45% by weight. Although solids-containing condensate was not removed from the plant, the gasification could be effected continuously for several months.
It will be appreciated that the instant specification and examples are set forth by way of illustration and not limitation, and that various modifications and changes may be made without departing from the spirit and scope of the present invention.

Claims (4)

What is claimed is:
1. The process for the production of gas from coal which comprises the steps of:
(a) effecting gasification by contacting a packed bed of coal with oxygen and water vapor at a pressure in the range of about 5-150 bars to form a raw gas containing tar, solids and water at a temperature of about 400°-700° C.;
(b) cooling said raw gas to effect condensation of the tar and water by contacting it with a cooling liquid containing water at a temperature of about 160°-220° C., the condensate containing the solids;
(c) separating from the solids-containing condensate a heavy fraction enriched in high-boiling tar with a solids content of about 10-60%;
(d) passing said heavy fraction to a solids disintegrator wherein substantially all of the solids are reduced in size to a particle size substantially below about 2 mm;
(e) then recycling at least part of said heavy fraction from step (d) to the gasification step (a); and
(f) finally recycling the balance of said heavy fraction to the separation step of step (c).
2. A process according to claim 1, wherein the condensate which is recycled to the gasification stage is kept at a temperature above about 50° C.
3. A process according to claim 1, wherein the disintegration reduces the predominant part of the solids to a particle size below about 0.5 mm.
4. A process according to claim 1, wherein the disintegration reduces the predominant part of the solids to a particle size below about 0.5 mm, and the condensate recycled to the gasification stage and to the solids-enriched fraction separation is kept at a temperature above about 70° C.
US05/840,433 1976-02-26 1977-10-07 Treating condensate from gasification of coal Expired - Lifetime US4187080A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US05/840,433 US4187080A (en) 1976-02-26 1977-10-07 Treating condensate from gasification of coal

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE2607745A DE2607745C2 (en) 1976-02-26 1976-02-26 Process for treating condensate from the cooling of raw gas from the pressurized gasification of solid fuels
DE2607745 1976-02-26
US70425376A 1976-07-12 1976-07-12
US05/840,433 US4187080A (en) 1976-02-26 1977-10-07 Treating condensate from gasification of coal

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US70425376A Continuation 1976-02-26 1976-07-12

Publications (1)

Publication Number Publication Date
US4187080A true US4187080A (en) 1980-02-05

Family

ID=27186764

Family Applications (1)

Application Number Title Priority Date Filing Date
US05/840,433 Expired - Lifetime US4187080A (en) 1976-02-26 1977-10-07 Treating condensate from gasification of coal

Country Status (1)

Country Link
US (1) US4187080A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4482363A (en) * 1982-02-15 1984-11-13 Shell Oil Company Process for the cooling and separating of small particle-containing gases
JPS6137931A (en) * 1984-07-27 1986-02-22 Ube Ind Ltd Separation of heavy metal from carbonous ash
WO2013188917A1 (en) * 2012-06-19 2013-12-27 Linc Energy Ltd Solution for coal condensate

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2142406A (en) * 1934-12-27 1939-01-03 Ici Ltd Apparatus for the wet purification of gases
US2657124A (en) * 1948-12-30 1953-10-27 Texas Co Generation of heating gas from solid fuels
US2799565A (en) * 1953-01-13 1957-07-16 Ruhrgas Ag Process for preventing or reducing the entrainment of fine solid particles in the gas stream of a gas producer
US3396514A (en) * 1966-11-07 1968-08-13 Babcock & Wilcox Co Gas cleaning system
US3540867A (en) * 1966-05-20 1970-11-17 Metallgesellschaft Ag Production of carbon monoxide and hydrogen
US3607157A (en) * 1969-07-23 1971-09-21 Texaco Inc Synthesis gas from petroleum coke

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2142406A (en) * 1934-12-27 1939-01-03 Ici Ltd Apparatus for the wet purification of gases
US2657124A (en) * 1948-12-30 1953-10-27 Texas Co Generation of heating gas from solid fuels
US2799565A (en) * 1953-01-13 1957-07-16 Ruhrgas Ag Process for preventing or reducing the entrainment of fine solid particles in the gas stream of a gas producer
US3540867A (en) * 1966-05-20 1970-11-17 Metallgesellschaft Ag Production of carbon monoxide and hydrogen
US3396514A (en) * 1966-11-07 1968-08-13 Babcock & Wilcox Co Gas cleaning system
US3607157A (en) * 1969-07-23 1971-09-21 Texaco Inc Synthesis gas from petroleum coke

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4482363A (en) * 1982-02-15 1984-11-13 Shell Oil Company Process for the cooling and separating of small particle-containing gases
JPS6137931A (en) * 1984-07-27 1986-02-22 Ube Ind Ltd Separation of heavy metal from carbonous ash
JPH0369387B2 (en) * 1984-07-27 1991-10-31 Ube Industries
WO2013188917A1 (en) * 2012-06-19 2013-12-27 Linc Energy Ltd Solution for coal condensate

Similar Documents

Publication Publication Date Title
EP0278063B1 (en) Process for upgrading water used in cooling and cleaning of raw synthesis gas
US4113615A (en) Method for obtaining substantially complete removal of phenols from waste water
AU661176B2 (en) Integrated carbonaceous fuel drying and gasification processand apparatus
US4199327A (en) Process for gasification of coal to maximize coal utilization and minimize quantity and ecological impact of waste products
CN1928027A (en) Method and device for producing synthesis gases by partial oxidation of slurries prepared from fuels containing ash and full quenching of the crude gas
US4465496A (en) Removal of sour water from coal gasification slag
US20080141591A1 (en) Gasification of sulfur-containing carbonaceous fuels
US3715301A (en) Multi-hydrotorting of coal
US4295864A (en) Process of treating pressurized condensate
US3715195A (en) Multihydrotorting of coal
US3840353A (en) Process for gasifying granulated carbonaceous fuel
DE2512317A1 (en) METHOD OF PRODUCING SYNTHESIS GAS
EP1432779B1 (en) Method and apparatus for the gasification of fuel in a fluidised bed reactor
SU704462A3 (en) Method of fuel gasifying
US4187080A (en) Treating condensate from gasification of coal
US4556402A (en) Process of gasifying solid fuels in a moving bed and in a fluidized bed
US4322221A (en) Process for the superatmospheric gasification of solid carbonaceous materials
CN86104274A (en) Remove prussic acid, ammonia and carbon oxysulfide in the synthetic gas
EP1137591B1 (en) Partial oxidation process with soot filter cake recovery
CA1194696A (en) Ash removal and synthesis gas generation from coal
US4217201A (en) Integrated coal cleaning, liquefaction, and gasification process
US4159897A (en) Producing fluid fuel from coal
GB1517140A (en) Process for producing a gas which has a high calorific value and a low dust content
US4089659A (en) Process for producing a lean gas by the gasification of a fuel mainly in lump form
US4099932A (en) Conversion of solid fuels to fluid fuels